Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1430804생성일: 2026년 10월 25일
Lithium Hexamethyldisilazide → 7-bromo-N-cyclopropyl-N-(4-methoxybenzyl)-2-(methylthio)imidazo[2,1-f][1,2,4]triazin-4-amine
https://huagongshe.com/reaction/1430804
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | N-((4-methoxyphenyl)methyl)cyclopropanamine | HCID 4721289 | — |
| 반응물 | 7-Bromo-2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazine | HCID 57457644 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-bromo-N-cyclopropyl-N-(4-methoxybenzyl)-2-(methylthio)imidazo[2,1-f][1,2,4]triazin-4-amine | HCID 86708490 | 72.7% |
반응 단계
To a 25 mL flask was added a mixture of 7-bromo-2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazine (2.0 g, 6.87 mmol), N-(4-methoxybenzyl)cyclopropanamine (1.34 g, 7.56 mmol) in anhydrous THF (20 mL). The reaction solution was cooled to −78° C. and treated dropwise with 1.0 M lithium bis(trimethylsilyl)amide in THF solution (20.61 mL, 20.61 mmol, 3 eq, 1M solution in THF). The reaction was stirred at −78° C. for 1 hour, then allowed to come to room temperature and stirred for 3 hours The reaction was quenched with saturated ammonium chloride. The product was extracted with ethyl acetate, the organic layer was dried with sodium sulfate and concentrated in vacuo. The crude product mixture was purified via ISCO (0-100% of ethyl acetate/heptane in 10 minutes, 24 g silica column) to give the pure product 7-bromo-N-cyclopropyl-N-(4-methoxybenzyl)-2-(methylthio)imidazo[2,1-f][1,2,4]triazin-4-amine (2.1 g)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08940736B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-7a1a5621a2574bd2ba679a66047b6b06 |
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| 출처 메모 | uspto-grants-2015_01 |
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